A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17049236



Internal ID100714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110828770..110833221hg38UCSC Ensembl
chr11:110699493..110703944hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384452
hg194452
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507585
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17049236
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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